WIREGRID MONITOR DEVICE

Description

FIELD OF INVENTION

[0001] The present invention relates to the field of biosensors and more specifically to a sub-diffraction-limited biosensor.

BACKGROUND OF THE INVENTION

[0002] Biosensor technology is well known in the art.

[0003] US Patent Application No.2003/0174992 discloses a method and an apparatus for providing a zero-mode waveguide including an analyte, which is subjected to activation by electromagnetic radiation for analysing the analyte.

[0004] WO 2006/136991 entitled "Luminescence sensors using sub-wavelength apertures or slits", discloses a biosensor with sub-wavelength spatial resolution.

[0005] WO 2007/072415 entitled "Luminiscence sensor operating in reflection mode", discloses a method for detection of fluorescent radiation generated by molecules in an aperture.

[0006] Such a biosensor may comprise a non-transparent material arranged on a substrate of a transparent material and forming at least one aperture for being filled with said analyte fluid. The apertures have a first in-plane dimension below the diffraction limit of the excitation light in the medium inside the apertures and a second in-plane dimension above the diffraction limit of the the excitation light in the medium inside the apertures. The aperture-plane is defined by a first vector directed along the first in-plane dimension of the aperture and a second vector directed along the second in-plane dimension of the aperture. Such a wire grid has a transmission axis where light that is polarized, such that the electric field is parallel with a transmission-plane, that is defined by the first vector and a third vector that is normal to the aperture-plane, below called T polarized light, is essentially transmitted and light that is polarized such that the electric field is orthogonal to the transmission-plane, below called R polarized light, is substantially blocked.

[0007] An analyte is applied to the biosensor and penetrates into the apertures. The analyte comprises a target molecule to be analyzed. The target molecule is labeled with a luminophore and the aggregate of luminophores/target molecule is immobilized at a substrate side of the apertures while free luminophores and luminophores attached to target molecules are present at an analyte side of the apertures in the analyte. The immobilized luminophores correspond to a qualitative or quantitative representation of the target molecule to be analysed.

[0008] Emission radiation from the immobilized luminophores is determined by a detector. In order to discriminate the desired radiation of the immobilized luminophores from background radiation of the free luminphores and the target molecules labeled with a luminophores, the background radiation has to be suppressed. The background radiation may be several orders of magnitude larger than the useful radiation from the immobilized luminophores. The substantial suppression of the luminescent background radiation enables essentially background free measurements that would otherwise require rinsing, but rinsing may not take place for example during real-time measurements. For a practical wire grid biosensor illuminated with polarized excitation light, the suppression of background radiation is limited to about three orders of magnitude. This limited background suppression, ultimately results in a reduction in the accuracy and surface-specificity of the sensor. Furthermore, there is a need in the art for a biosensor that can use a non-polarized light source, such as a light emitting diode, LED, which is cheaper and may produce a larger output power.

[0009] Document WO2007010428 discloses a luminescence sensor, such as e.g. a luminescence biosensor, comprising a multi-layer structure. Document WO2006135782 discloses an apparatus, a system and a method for detecting separately and substantially simultaneously light emissions from a plurality of localized light-emitting analytes. This document discloses an array of sub-wavelength slits illuminated by excitation light polarized perpendicular to the transmission plane of the slits. The excitation light is incident from the same side of the detector with a given angle, to make sure that reflected excitation light does not reach the detector. Wenger et al ("Single molecule fluorescence in rectangular nanoapertures", optics express opt. Soc. America usa, vol. 13, no. 17,

[0010] August 2005) describe how Fluorescence Correlation Spectroscopy is used to investigate fluorescent molecules in solution diffusing in subwavelength rectangular apertures milled in Aluminium films. Document WO2007072293 discloses a method and a sensor for the detection of luminescence radiation generated by at least one luminophore. This document discloses a device including a biosensor with apertures (slits), sub-wavelength in one dimension, and a polarizer for blocking radiation polarized parallel to the transmission plane of the apertures. The biosensor is illuminated by polarized excitation light from the other side with respect to the detector. The polarizer suppresses the excitation light before it reaches the detector.

SUMMARY OF THE INVENTION

[0011] The invention is defined by the device of independent claim 1. Preferred embodiments are defined by the dependent claims.

BRIEF DESCRIPTION OF THE DRAWINGS

[0012] Further objects, features and advantages of the invention will become apparent from the following detailed description of embodiments of the invention with reference to the drawings, in which:

Fig.1 is a schematic illustration for explaining the principles;

Fig.2 is a schematic illustration of an embodiment of a biosensor;

Fig.3 is a schematic illustration of another embodiment of a biosensor; and

Fig.4 is a schematic illustration of a further embodiment of a biosensor

Fig.5 is a schematic block diagram of an embodiment of the invention;

Fig.6 is a schematic block diagram of an example outside the scope of the invention;

Fig.7 is a schematic block diagram of a further example outside the scope of the invention;

Fig.8 is a schematic block diagram of a still another example outside the scope of the invention;

Fig.9 is a schematic block diagram of a yet another example outside the scope of the invention;

Fig.10 is a schematic block diagram of a still yet another example outside the scope of the invention;

Fig.11 includes two photographs showing a detector picture with a polarization filter arranged in parallel with and perpendicular, respectively, to a wiregrid that is covered with a pattern of labelled molecules.

DETAILED DESCRIPTION OF EMBODIMENTS

[0013] Below, several examples will be described with references to the drawings. These embodiments are described in illustrating purpose in order to enable a skilled person to carry out the invention and to disclose the best mode. However, such embodiments do not limit the invention. Moreover, other combinations of the different features are possible within the scope of the invention.

[0014] A biosensor according to the embodiments described below may comprise an analyte arranged in apertures defined in a material that is non-transparent for at least one of the exitation and the luminescence light, typical examples are Aluminum, Gold, Silver, Chromium, having a first in-plane dimension below the diffraction limit of the excitation light in the medium inside the apertures and a second in-plane dimension above the diffraction limit of the excitation light in the medium inside the apertures. By in-plane dimension is meant the dimension in a plane parallel to the substrate.

[0015] The analyte may be included in a fluid. A luminophore present in the fluid will emit electromagnetic radiation when exposed to excitation energy. The emitted radiation is collected by a detector.

[0016] The total emitted radiation energy, i.e. the sum of the radiation energy of the individual luminophores emitted by the luminophores, has a predetermined relationship to a property of the analyte such as being proportional to a concentration of a molecule of the analyte. By analysing the emitted radiation, properties of the analyte can be determined, quantitatively and/or qualitatively.

[0017] A method for immobilizing analyte molecules at the bottom of each aperture will be described herein-after. Each analyte molecule is provided with a luminophore, such as a fluorescent label. By exciting the luminophore and collecting the emitted radiation, a detection of the analyte molecule may be provided. The detection can be qualitative and/or quantitative.

[0018] Ligands or capture molecules may be arranged or immobilized at specific portions of the aperture, said ligands forming luminophores when contacted by a target molecule of the analyte. Such formation of luminophores may take place in different manners, such as described in the article: "Fluorescence spectroscopy of single biomolecules" by S. Weiss, Science, Vol. 283, pp 1676-1683, the technical contents of which are hereby incorporated by reference. The ligands may immobilize the luminophores so that they emit radiation from the immobilized positions at excitation.

[0019] The ligands may be immobilized in trenches arranged in a substrate adjacent to the bottom of the apertures.

[0020] The luminophores may be excited to emit radiation in different manners, such as by electric or chemical energy. The emitted radiation may take place by different physical processes, such as luminescence, phosphorescence, fluorescence, Raman scattered light, Hyper-Raman scattered light or Hyper-Rayleight scattered light etc. The emitted radiation may be electromagnetic radiation, such as light, including infrared light.

[0021] Luminophores which are excited with electromagnetic radiation will be considered, specifically light, including ultraviolet, visible and infrared light, with a wavelength in the relevant medium that is at least twice as large as the first in plane dimension of the aperture. The effective wavelength is the wavelength of the radiation in vacuum divided by the refractive index of the medium.

[0022] The luminescent radiation emitted by the luminophore can be detected at either side of the biosensor. If the analyte fluid is present on a front side, the radiation can be detected at a back side of the substrate. When a light source is directed towards the substrate from the back side thereof, R-polarized excitation light will establish an evanescent field inside the apertures, while T-polarized excitation light will establish a propagating wave inside the aperture. Such an evanescent field may excite the luminophores present in the aperture adjacent the substrate side. The evanescent field will have an exponential decay in the aperture from the substrate side of the aperture. Thus, luminophores present close to the substrate side of the aperture will be more efficiently excited than luminophores present at or outside the analyte side of the aperture. Excitation light which is non-polarized or with other polarization states, such as circularly, elliptically, or linearly polarized light that is a linear combination of R and T polarized light, can be decomposed into R and T polarized light and will result in a combination of evanescent and progating excitation light inside the aperture.

[0023] The generated luminescent radiation will in general have a polarization state with both R and T polarized components. The T polarized fraction of the luminescent light will be essentially transmitted by the aperture, while the R polarized component will be substantially suppressed by the aperture.

[0024] In many applications, a background attenuation of about 1000 would be sufficient, but one would rather use a non-polarized light source, such as a light emitting diode, LED, which is typically less expensive than a laser and may still provide the required excitation power.

[0025] Fig. 1 discloses a system according to a first example. The system comprises a wiregrid biosensor, for example of the type disclosed in WO 2007/072241.

[0026] The biosensor 1 comprises several "wires" 3 arranged on a transparent substrate 2. The substrate may be made from glass, silica or other similar material, such as acrylic glass, epoxy resin, polyvinylchloride (PVC), etc. In order to be sufficiently transparent, the material should have a refractive index with an imaginary part smaller than 10^-4. The wires may be formed by a metal, such as gold, aluminium, silver, chromium, etc, which is etched or plated to obtain the desired structure, i.e. the plurality of apertures 4. Formation of such wires and a wiregrid is known in the art, see for example WO 2006/136991.

[0027] A plurality of apertures 4 are formed between the wires 3. The aperture has a sub-diffraction-limited dimension in a first in-plane direction. This first in-plane dimension is smaller than half the effective wavelength of the excitation radiation. If water (n=1.3) is present in the aperture and the excitation radiation has a wavelength in vacuum of 633 nm, the effective wavelength will be 487 nm and the first in-plane dimension of the apertures is smaller than half the effective wavelenght being 243 nm. The first in-plane dimension may be smaller than 0.25 times the effective wavelength or 121 nm. The first in-plane dimension may be smaller than 0.2 times the effective wavelenght or 97 nm. The first in-plane dimension may be smaller than 0.15 times the effective wavelenght or 73 nm. The second in-plane dimension of the aperture is larger than half the effective wavelength, such as at least 0.5 times the effective wavelength or at least 243 nm. The second in-plane dimension may be 10 to 100 times the effective wavelength, or 4.9 to 49 µm. The second in-plane dimension may be 100 to 1000 times the effective wavelength, or 49 to 490 µm. The second in-plane dimension may be at least 1000 times the effective wavelength, or at least 490 µm.

[0028] An analyte fluid 5 may be introduced in the apertures of the biosensor. The analyte may comprise target molecules 7 provided with labels of a luminophore or fluorophore 8 that is able to emit electromagnetic radiation upon excitation.

[0029] The substrate 2 may be provided with capture molecules or ligands 6 that exhibit an affinity towards the target molecules 7 and being immobilized at the surface of said substrate 2 at the bottom or substrate side of the aperture. When a target molecule 7 comes sufficiently close to a ligand 6, the target molecule is caught by the ligand and forms an aggregate 9 comprising a ligand 6, a target molecule 7 and a fluorophore 8. The target molecule and the label or fluorophore attached thereto becomes immobilized at a position close to the substrate side of the aperture 4.

[0030] The biosensor 1 is exposed to excitation radiation 10 from an external radiation source, comprising for example light at a wavelength of about 700 nm. Other wavelength radiation may be used as well such as microwaves, infrared light, near-infrared (NIR) light, visible light, ultraviolet ligth, X-ray, etc.

[0031] In case of circularly polarized light, the excitation radiation can be decomposed into (about) 50% T- and (about) 50% R-polarized radiation. As a result (about) 50% of the excitation radiation is substantially transmitted and the other (about) 50% of the excitation radiation generates an evanescent field inside the aperture that decays exponentially and is essentially not transmitted. Substantial suppression of the excitation light for positions away from the sample facet of the wiregrid, therefore requires that the light is essentially R-polarized.

[0032] The biosensor may be operated in reflection mode. The biosensor is exposed to excitation radiation 10 directed towards the substrate end of the apertures.

[0033] The aggregate 9 comprising a fluorophore 8 immobilized adjacent the substrate side will absorb excitation energy and emit fluorescent radiation in all directions, depending on the direction of the transition dipole moment, the fluorescent is more or less pronounced in some directions, as indicated by arrows 11a and 11b. A portion 11a of the emitted radiation is directed towards a detector 12 arranged below the substrate 2, while another portion 11b is directed towards the analyte side of the aperture.

[0034] Even when properly polarized excitation light is used, a small fraction η of the excitation light (for a typical aperture as described above the transmitted R-polarized excitation light is a factor 1/1000 of the incident R-polarized excitation light 10) is transmitted by the aperture. This transmitted fraction η can be absorbed by fluorophores 8 present in the fluid 5 at the analyte side of the aperture and excite such fluorophores to emit radiation as indicated by arrows 14a and 14b. The emitted radiation has in general both T- and R-polarized components. The fluid may comprise free target molecules 7 provided with fluorophores 8, as well as free fluorophores 8. The portion of the radiation indicated by arrows 14a will pass through the aperture and the portion of such radiation that is T-polarized will, in contrast to R-polarized components be transmitted by the aperture and give rise to undesired background radiation.

[0035] If a large amount of external fluorophores 8 that are not bound to ligands 6 is present in the fluid 5 at the analyte side of the apertures, such background radiation will be large. Such external fluorophores may be reduced by rinsing, but rinsing may not take place for example during real-time measurements.

[0036] It is noted that, typically, the largest portion of the radiation 14a from fluorophores present in the fluid 5 at the analyte side and passing through the aperture at the substrate side, is T-polarized light. A small fraction, which is about 0.5*η, of the radiation 14a that passes the aperture is R-polarized light.

[0037] A polarization filter 33 is arranged before the detector 12. The polarizing filter has a high suppression, which is equal or better than the suppression 1/η of an aperture, such as more than 10,000 for T-polarized light. Thus, most of the radiation 14a from the fluorophores present in the fluid 6 will be blocked by the filter 33. Thus, the background radiation will be reduced by the factor between 0.5*η and η depending on the suppression of filter 33, which is a substantial reduction. The useful radiation, or the radiation to be detected 11a, will also be reduced, but only with a minor factor. Thus, an improvement of the signal-to-background ratio of between 0.5/η and 1/η has been obtained by means of the filter 33.

[0038] The filter 33 can have an attenuation factor of at least the same as said wiregrid attenuation factor η, but may have a still larger attenuation factor of more than about 10η. Such polarizing filters are commercially available, such as Glan-laser polarizers with a typical attenuation factor of 100000.

[0039] The polarization filter 33 may be a wiregrid similar to the biosensor 1, in which case the polarizing filter 33 has the same suppression η as the wiregrid. In this case, the suppression will only be 50% of the theoretically maximally obtainable improvement.

[0040] A further reduction of the background radiation may be obtained by using R-polarized excitation radiation. In this case, the excitation radiation will be attenuated when passing the aperture by said attenuation factor η, which means that the background radiation reaching the detector 12 will be reduced by a factor of 0.5*η^2 to η^2 depending on the attenuation factor of filter 33, i.e. in the case indicated above by a factor of 500,000.

[0041] The same polarizing filter 33 may be used for both the excitation radiation and for blocking background radiation to the detector, as indicated by broken lines 33a in Fig.1.

[0042] Excitation radiation reflected from the substrate 2 and the wiregrid would also reach the detector as background radiation. Such excitation background radiation can be reduced by different measures, such as filters passing only the fluorescent emitted radiation. The excitation radiation can also be directed towards the biosensor at an angle, so that the reflected radiation does not reach the detector. In this case, scattered excitation radiation directed towards the detector can be removed by a wavelength filter 37 that transmits the fluorescent radiation and blocks the excitation radiation.

[0043] Fig.2 discloses an embodiment, comprising a substrate 2 of glass provided with a wiregrid 3 of a metal, such as aluminum, gold, silver, chromium, etc. The wiregrid comprises apertures in the form of slits having a first in-plane dimension (width) less than the diffraction limited width 270nm, such as 70 nm. The slit has a second in-plane dimension (length), larger than the diffraction limited width, such as 1 mm. A target molecule having a fluorophore 20 is immobilized/binds at the substrate end of the aperture and another fluorophore 21 is present in a fluid 5 present at the analyte end of the aperture.

[0044] Excitation radiation, such as light having a wavelength in vacuum of about 700nm, indicated by arrows 10b, is directed from a source towards a dichroic mirror 31. From the dichroic mirror 31, the excitation radiation passes said polarization filter 33 to a lens 32 for focusing the polarized excitation radiation 10b towards the biosensor surface.

[0045] The excitation radiation influences the fluorophores to emit radiation. Emitted radiation 20a from fluorophore 20 present at the substrate side of the aperture will pass through the lens 32 and through the polarizing filter 33, passing only R-polarized radiation 20b. The passed radiation 20b will be reflected by the dichroic mirror 31 towards lens 34 and a detector 22.

[0046] The R-polarized excitation radiation 10b at the substrate side of the aperture forms an evanescent field inside the apertures having an exponential decay. The excitation radiation will be attenuated by said attenuation factor η and only a small fraction of the excitation radiation will reach the fluorophore 21 at the analyte side of the aperture. The fluorophore 21 will emit radiation 21 a, which will pass the aperture and reach the lens 32 and the polarizing filter 33. The T-polarized component 21b of the radiation from fluorophore 21 will pass the apertures, but will be blocked by the polarizing filter 33. The R-polarized component of the radiation from fluorophore 21 will be attenuated when passing the aperture by said attenuation factor η and will pass through lens 32, polarizing filter 33 and be directed by the dichroic mirror 31 towards the lens 34 and the detector 22. Thus, the background radiation from fluorophore 21 will be attenuated by a factor η^2 compared to the situation without the polarizing filter 33.

[0047] The polarizing filter 33 can be aligned with the wiregrid at the setup of the biosensor, by measuring the level of the excitation radiation at the analyte side of the apertures. When the this-way measured excitation radiation level is at minimum, the polarizing filter 33 is aligned with the wiregrid, meaning that the polarizing filter passes only radiation having a polarization perpendicular to the wiregrid.

[0048] By rotating the polarizing filter, the background reduction can be made variable. This improves flexibility, since orientation of the external polarizing filter can be rotated, which allows not only to suppress the background but also to measure the background and to determine the polarization state of the bound fluorophores.

[0049] Fig.3 discloses another embodiment, in which the polarizing filter 24 is only passed by the radiation emitted by the fluorophores. In this case, the polarizing filter 24 does not need to be transparent for the excitation radiation, which may be relevant for fluorophores with large Stokes shift, such as larger than 100nm. The excitation radiation may have a circular polarization. Alternatively, the excitation may be linearly-polarized radiation, in which case the polarization should be aligned as indicated above.

[0050] Fig.4 discloses a further embodiment, in which the polarizing filter 24 of the embodiment of Fig.3 is replaced by a polarizing beam splitter 35. The polarizing beam splitter 35 passes R-polarized radiation 20b to lens 34 and detector 22, while the polarizing beam splitter 35 directs T-polarized radiation 20c and 21b to a second lens 36 and a second detector 23. Thus, the background signal can be estimated.

[0051] Fig.5 shows an embodiment of the present invention including the biosensor 1, which is exposed to excitation radiation 10 from an external radiation source, comprising for example ultraviolet, visible or infrared light. The radiation source is included in a detection device 30, which is separate from the biosensor 1 defined above.

[0052] In the present embodiment, a non-polarized light source is used, such as one or several LED:s. Such a light source may emit larger power of excitation radiation and is much cheaper than a laser source.

[0053] The light source unit 40 comprises one or several LEDs 41 that emit radiation around a wavelenght of 630 nm, a lens 42 and a pass filter 43 for passing excitation light and for removing light that overlaps the emission band of the fluorescent labels and the pass band of emission filter 54. Thus, the filter may have a pass-band which is typicall 20 to 30 nm wide and transmits light 10 that overlaps the absorption or excitation band of the fluorescent labels. An example of a suitable passband wavelength range for these LEDs is 620 to 650 nm; a suitable pass filter is the 3RD Millenium 620-650 filter available from Omega Optical, Inc.

[0054] The light is directed towards the biosensor from the substrate side at an angle and the light is partially reflected by the wire grid, as shown by light beam 15. Thus, substantially no excitation light reaches a sensor 71. Only a small fraction of scattered excitation light is directed towards the sensor 71, as shown by broken lines 16.

[0055] An imaging block 50 is arranged at substantially right angle to the biosensor at the back side thereof. The imaging block 50 comprises a fist lens 51 and a second lens 52 for directing emission radiation 17 towards a detector 71 via a polarizer 53 and one or several emission filters 54, which pass emission radiation 17 and block excitation radiation 16, if any. For fluorescent labels such as atto-680 dye or Fluor 633 dye, which have emission spectra with a spectral width of about 50 nm centred around wavelength of 700 nm and 650 nm, respectively, suitable transmission wavelengths for the emission filters 54 have a minimum transmission wavelength of 660 nm or larger, such as the 695AF55 Emitter XF3076 filter available from Omega Optical, Inc, which has a minimum transmission wavelength of 665 nm.

[0056] The detector 71 may be a camera comprising a CCD or a CMOS detector. Further alternatives appear below.

[0057] In case of non-polarized light, the excitation radiation can be decomposed into T- and R-polarized radiation. As a result, about half of the excitation radiation is substantially transmitted through the wire grid and the other half of the excitation radiation generates an evanescent field inside the aperture that decays exponentially and is essentially not transmitted. Only a small fraction of the R polarized radiation will pass through the aperture. Thus, the wire grid operates substantially as a polarization filter.

[0058] The ratio between the radiation passing the wire grid and the radiation impinging on the wire grid is called the extinction rate, and is typically about 0.001 for R polarized radiation for a typical wiregrid.

[0059] The radiation will excite the fluorescent labels to emit fluorescent radiation. For an ensemble of fluorophores, the labels may emit about 75% of the same polarization as the excitation radiation polarization.

[0060] The fluorescent labels 61 positioned in the aperture adjacent to the substrate end of the aperture is excited by excitation radiation having T and R polarization, wherein T normally is approximately equal to R for unpolarized excitation light. The total excitation radiation is T+E which results in a fluorescent emission from the labels. The emission will be in all directions and it is asumed that 50% will be directed towards the detector.

[0061] A fluorescent label 62 positioned outside the aperture adjacent to the front side or sample side of the biosensor will be excited by the T component of the excitation light which passes the wire grid almost unattenuated. In addition, the R component of the excitation light will be attenuated by the extinction factor n. Thus, the T component and the R component will result in emission radiation. This emission will be in all directions and it is assumed that 50% will reenter into the aperture towards the detector. However, the R component will be attenuated by the extinction factor n. Finally, the polarization filter will reduce the T component by a factor N. The ratio between the detected fluorescence that originate from labels 61 and 62 after the polarization filter is:

[0062] If it is assumed that N=n, than the ratio will be 1/n, which demonstrates that the first embodiment of the present invention results in a background suppression similar to the extinction ratio of a wire grid. If N«n, the ratio will be about 4/n. A typical extinction ratio of a wiregrid is n=0.001.

[0063] The polarization filter 53 can have an extinction factor N of at least the same as said wiregrid extinction factor n, but may have a still smaller extinction factor of less than about 0.1 *n. Such polarizing filters are commercially available, such as Glan-laser polarizers with a typical extinction factor of 10^-5.

[0064] The polarization filter 53 may be a wiregrid similar to the wiregrid 1, in which case the polarizing filter 53 has the same extincton factor n as the wiregrid.

[0065] Excitation radiation scattered from the substrate 2 and the wiregrid would also reach the detector as background radiation. Such excitation background radiation is reduced by emission filter 54, which attenuates light with a wavelength shorter than the emission wavelenght, and thus essentially blocks the excitation light.

[0066] The embodiment according to Fig.5 operates in reflection mode, in which the light source and the detector both are arranged at the back side of the biosensor and the fluid to be detected is on the opposite side of the wires on the substrate. The light is directed towards the substrate with an angle larger than the numerical aperture of the first lens 51 in order to be reflected in another direction than towards the detector.

[0067] Fig.6 discloses an example outside the scope of the invention with a wire grid having apertures similar to the first embodiment, operating in transmission mode, in which the light source is arranged at the front side of the biosensor and the detector is arranged at the back side of the biosensor. The operation is similar to the embodiment according to Fig.5.

[0068] Light emitted by the LED 41 is focused by a lens 42 and illuminates an aperture or a plurality of apertures of the grid after passing the pass filter 43. The excitation light having T polarization will pass the aperture essantially unattenuated, while the excitation light having R polarization will be substantially blocked.

[0069] The excitation light passing through the aperture will essentially be T polarized excitation light, which is substantially blocked by the polarization filter 53. Any T polarized excitation light still passing through the polarization filter 53, and attenuated by the extinction rate N, and any R polarized excitation light still passing the wiregrid, and attenuated by the extinction rate n, will be blocked by the pass filter 54, which may comprise several cascaded filter, before reaching the detector 71.

[0070] The fluorescent label 61 positioned at the substrate end of the aperture will be excited substantiall only by the T component of the excitation light, which means that it will emit about half of the emission radiation of the first embodiment in Fig.5.

[0071] The background label 62 positioned outside the aperture adjacent to the sample end of the aperture will emit emission radiation. The T component will pass and the R component will be reduced by the extinction factor n.

[0072] Thus the ratio between the emission of the substrate end label 61 and the sample end label 62 reaching the detector will be:


If N=n, and n<<1 (typical value for n=0.001), the ration will be about 1/(8*n). If n<<1, and N«n (that is a polarizer 53 with an extinction ratio substantially smaller than the wire grid), the ratio will be about 1/(4*n).

[0073] In another example, the excitation radiation is directed towards the wiregrid essentially parallel to the substrate, as shown in Fig.7. A dicroic mirror 91 is arranged in the light path of, for example, the LED light and redirect the light perpendicular towards the substrate. The dicroic mirror is designed to reflect the excitation light at wavelength 620 to 650 nm and pass emission light at wavelengths larger than 670 nm. Thus, the emission filter 54 may be dispenced with as indicated in Fig.7, but the emission filter 54 may be included if the dicroic mirror still passes a small fraction of the excitation light.

[0074] The polarizing filter 53 can be aligned with the wiregrid at the setup of the biosensor, for example by illumination of the wiregrid from the sample-end (i.e. via the fluid on top) and minimizing the power on the detector 71. When the this-way measured power is at minimum, the polarizing filter 53 is aligned with the wiregrid, i.e. arranged perpendicular to the wiregrid, meaning that the polarizing filter passes only radiation having R polarization perpendicular to the plane of transmission of the wiregrid.

[0075] By rotating the polarizing filter, the background reduction can be made variable. This improves flexibility, since orientation of the external polarizing filter can be rotated, which allows not only to suppress the background but also to measure the background and to determine the polarization state of the bound fluorophores.

[0076] Fig.8 discloses a further example, in which the polarizing filter 93 is arranged in another position compared to the embodiment of Fig.5, namely between the imaging block 50 and the substrate 2. In addition, the polarizing filter 93 is arranged between the light unit 40 and the substrate so that the light from the LED:s 41 passes the polarization filter 93 before reaching the substrate. Thus, the excitation light from the LEDs to the substrate and the emission light from the fluorescent labels passes through the same polarizing filter 93. The polarzising filter is arranged in such a position that the excitation light being non-polarized passes through the polarization filter 93, which passes R polarized radiation but attenuates T polarized radiation by a factor N, which may be 10^-3 to 10^-6. The fluorescent label 61 positioned at the substrate end of the aperture and the fluorescent label 62 positioned at the sample end of the aperature will emit emission radiation. When passing back through the aperture, the R component will be further attenuated by a factor n, and when passing through the polarization filter, the T component will be attenuated by a factor N. The ratio between the emission radiations from label 61 and label 62 after the polarization filter is:




If N=n, the ratio will be 3/(8*n*n)
If N«n, the ratio will be about 1/(n*n).

[0077] The polarization filter 93 is arranged with the polarization direction perpendicular to that of the wiregrid. If the polarization filter 93 is a wiregrid, the grid direction of the filter should be perpendicular to the grid direction of the wiregrid.

[0078] As shown in Fig.9, the polarization filter 53 of the embodiment of Fig.7 can be replaced by a polarizing beam splitter 92. The polarizing beam splitter 92 passes R polarized radiation 18 to the detector 71, while the polarizing beam splitter 92 directs T-polarized radiation 19 on to a second detector 94. Thus, the background signal can be measured. The polarizing beam splitter 92 may replace the polarization filter 53 also in the embodiments according to Figs. 1 and 2.

[0079] Fig.10 shows a further example, similar to Fig.7 or Fig.9, in which the polarization filter is arranged in the same position as in the embodiment of Fig. 8, i.e. close to the substrate. Thus, excitation light from the un-polarized light sourde 41 is directed towards the dicroic mirror 91 and reflected towards the substrate via the polarization filter 93, which substantially only passes R polarized radiation. The excitation radiation results in fluorescence emission radiation from the fluorophore label 61, which passes through the polarization filter 93, the dicroic mirror 91 to the detector 71, and from the fluorophore label 62, which passes through aperture, the polarization filter 93, the dicroic mirror 91 to the detector 71. The calculation of the ratio between the emission radiations from the fluorescent labels 61 and 62 is the same as for the embodiment of Fig.8.

[0080] In the above-mentioned embodiments, a wiregrid biosensor of a simple and cheap construction can be used, which means that the wiregrid can be disposable.

[0081] The polarizing filter is arranged outside the biosensor and can be used several times. The polarizing filter is arranged without contact with the analyte to be examined. The polarizing filter is always arranged between the transparent substrate and the sensor. Thus, a more versatile polarizing filter can be used, resulting in a very large background radiation attenuation, without substantially increasing the total cost per analysis.

[0082] The different elements of the light source unit 40 and the imaging block 50 can be arranged in other orders than indicated above. Thus, the excitation radiation pass filter 43 can be arranged between the light source 41 and the lens 42. In the embodiment of Fig.7, the dicroic mirror can be arranged to perform the operation of the pass filter 43, which becomes superfluous and can be dispenced with. In the imaging block 50, the elements order can be different. For example, the polarization filter may be arranged in any position between the substrate and the detector 71.

[0083] The embodiment of the invention according to Fig.5 was used in a test environment having the following properties:

In order to demonstrate the background suppression, samples with a honeycomb pattern of labelled proteins have been fabricated by sputtering a chess board pattern of SiO2 spacer material on the wire grid, followed by immobilization of proteins labelled with Fluor 633 dye on the portions of the transparent substrate 2 that overlap with the apertures 4 and that are not covered by the spacer material. On top of the fabricated samples were attached 0.5 mm thick hybridization chambers filled with a very high concentration, such as 4.5 micro molar, of a dye solution, such as atto-680 dye, available from available from Atto-Tec GmbH. These samples were characterized in a set-up similar to the set-up of Figure 1, using 4 red LEDs spectrally filtered to limit the excitation wavelengths between 620 to 650 nm. By rotating the transmission axis of the polarizer, it was possible to switch the detection volume from essentially evanescent or near field to essentially the complete hybridization chamber.

[0084] Fig.11 shows the measured fluorescence images: To the left, the measured fluorescence images for the polarizer being parallel to the transmission axis of the wiregrid and to the right for the polarizer to be orthogonal to the transmission axis of the wire grid. The detection volume was limited to essentially only the labelled proteins on the substrate-end of the aperture and a small evanescent volume of dye solution with a height of only 20-30 nm. Integration time for the left image is about a factor 500 smaller than for right image. From Figure 11, it can be clearly seen that the background generated by the fluorescent fluid on top of the wire grid can efficiently be suppressed The fact that the integration time for the left image is about a factor 500 smaller, clearly demonstrates that it is possible to suppress background fluorescence that is substantially larger than the signal.

[0085] Moreover, in the embodiment according to Fig.5, dark field illumination of the wire grid is used where the angle of incidence of the incident light is larger than the angle corresponding with the numerical aperture of the collection lens used for imaging on the detector. This way, the specularly reflected light is not imaged on the detector.

[0086] The present embodiments have one or several of the following advantages:

Critical alignment between polarization axis of excitation source and transmission axis of wire grid is no longer required. In previous embodiments, the polarization axis of source has to be aligned orthogonal to the transmission axis of the wire grid to generated a purely evanescent field in the space between the wires.

[0087] Lasers are typically more expensive than un-polarized sources. For applications such as fluorescence, the absorption band of the label molecules is quite wide and this allows the use of LEDs. LEDs are especially attractive because they offer similar power levels as lasers at a substantially lower cost. Furthermore it is anticipated that the optical powers of LED will substantially increase in the future.

[0088] Polarization purity of a typical laser is 100:1, while typical extinction of wire grids used in wire grid biosensor concept is better than 1000. This implies that each laser requires a dedicated polarizer with extinction equal to or better than the extinction of the wire grid.

[0089] Long coherence length of a laser implies speckle and this limits uniformity of illumination. In the present embodiments, there is used a light source having low coherence length, such as a bandwith larger than 1 nm (please review this portion).

[0090] The embodiments can be used in different applications, such as an optical biosensor for measurement with high surface specificity as required for measurement in high background environment, e.g. DNA-hybridization assay with high multi-plex number.

[0091] The embodiments can be used as a microscope, wherein the sensor 71 essentially is replaced by the eye of the user.

[0092] Although the present invention has been described above with reference to specific embodiment, it is not intended to be limited to the specific form set forth herein. Rather, the invention is limited only by the accompanying claims and, other embodiments than the specific above are equally possible within the scope of these appended claims.

Claims

1. A device for monitoring radiation emitted by luminophores present in an analyte fluid, comprising:

a biosensor having at least one non-transparent material (3) arranged on a substrate of a transparent material (2) and forming at least one aperture (4) for being filled with an analyte fluid, wherein said aperture has a first in-plane dimension, which is smaller than half an effective wavelength of radiation in the biosensor and a second in-plane dimension which is larger than half an effective wavelength of the excitation radiation, and has a plane of transmission;

luminophores immobilized adjacent the substrate side of the aperture that are able to generate a radiation to be detected and luminophores present at or outside the analyte side of the aperture that are able to generate an undesired background,

an excitation source (10,41) configured to emit an excitation radiation which is non-polarized or circularly, elliptically or linearly polarized as a linear combination of evanescent and propagating excitation light inside the aperture for exciting the luminophores present in the analyte fluid of said biosensor;

an imaging block (50) comprising a detector (71) for detecting radiation emitted by the luminophores upon excitation, and a lens (51) for directing radiation emitted by the luminophores towards detector (71), said imaging block (50) arranged at a substrate side of the biosensor;

and a polarizing filter (53) arranged in the optical path of the radiation emitted by said luminophores between the biosensor and the detector and outside the optical path of the excitation radiation, said polarizing filter being configured to substantially suppress the polarization component of the radiation emitted by said luminophores which is parallel to the transmission plane of the aperture;

wherein the excitation radiation is directed toward the biosensor from the substrate side at an angle larger than the numerical aperture of lens (51), in order to be reflected in another direction than towards the detector.

2. The device according to any one of the previous claims, wherein said polarizing filter (33,53) is rotatable.

3. The device according to claim 1 or 2, wherein said light source (41) comprises a band pass filter (43) for passing radiation having a wavelength pass band corresponding to an absorption wavelenght band for excitation of said luminophores, and for blocking radiation having a wavelength corresponding to an emission wavelength of said luminophores.

4. The device according to claim 3, wherein a wavelength pass filter (54) is arranged before the detector (71) for passing radiation having a wavelength corresponding to an emission wavelength of said luminophores and blocking radiation passed by said band pass filter (43).

5. The device according to any one of the previous claims, wherein the polarizing filter comprises a polarizing beam splitter (92) passing radiation having a polarization plane orthogonal with the transmission plane of the aperture towards said detector (71), and reflecting or blocking radiation having a polarization parallel to the transmission plane of the aperture towards a second detector (94).

6. The device according to any one of claims 1 to 5, wherein said light source emits light having a low coherence length, such as having a bandwith larger than about 1 nm.

7. The device according to any one of the previous claims, wherein a capture molecule is arranged adjacent a substrate end portion of the aperture, said capture molecule being intended to form an aggregate with said target molecule and luminophore.

Ansprüche

1. Vorrichtung zur Überwachung von Strahlung, die durch in einem Analytfluid anwesende Luminophore emittiert wird, wobei die Vorrichtung Folgendes umfasst:

einen Biosensor mit mindestens einem nicht-transparenten Material (3), das auf einem Substrat aus einem transparenten Material (2) angeordnet ist und mindestens eine Apertur (4) zum Füllen mit einem Analytfluid bildet, wobei die genannte Apertur eine erste Dimension in der Ebene hat, die kleiner ist als die Hälfte einer effektiven Wellenlänge der Strahlung in dem Biosensor, und eine zweite Dimension in der Ebene hat, die größer ist als die Hälfte einer effektiven Wellenlänge der Anregungsstrahlung, und eine Transmissionsebene hat;

angrenzend an die Substratseite der Apertur immobilisierte Luminophore, die in der Lage sind, eine zu detektierende Strahlung zu erzeugen, und an oder außerhalb der Analytseite der Apertur vorhandene Luminophore, die in der Lage sind, einen unerwünschten Hintergrund zu erzeugen;

eine Anregungsquelle (10, 41), die konfiguriert ist, um eine Anregungstrahlung zu emittieren, die nicht-polarisiert oder kreisförmig, elliptisch oder linear polarisiert ist als eine lineare Kombination von abklingendem und sich ausbreitendem Anregungslicht innerhalb der Apertur, um die in dem Analytfluid des genannten Biosensors anwesenden Luminophore anzuregen;

einen Bildgebungsblock (50), der einen Detektor (71) zum Detektieren der auf die Anregung hin durch die Luminophore emittierten Strahlung und eine Linse (51) zum Lenken der durch die Luminophore emitterten Strahlung auf den Detektor (71) umfasst, wobei der genannte Bildgebungsblock (50) an einer Substratseite des Biosensors angeordnet ist;

und einen Polarisationsfilter (53), der in dem optischen Pfad der durch die genannten Luminophore emittierten Strahlung zwischen dem Biosensor und dem Detektor und außerhalb des optischen Pfads der Anregungsstrahlung angeordnet ist, wobei der genannte Polarisationsfilter konfiguriert ist, um im Wesentlichen die Polarisationskomponente der durch die genannten Luminophore emittierten Strahlung zu unterdrücken, die pararllel zu der Transmissionsebene der Apertur verläuft;

wobei die Anregungsstrahlung von der Substratseite aus in einem Winkel, der größer ist als die numerische Apertur der Linse (51), auf den Biosensor gelenkt wird, um in einer anderen Richtung als zum Detektor hin reflektiert zu werden.

2. Vorrichtung nach einem der vorhergehenden Ansprüche, wobei der genannte Polarisationsfilter (33, 53) drehbar ist.

3. Vorrichtung nach Anspruch 1 oder 2, wobei die genannte Lichtquelle (41) einen Bandpassfilter (43) hat, um Strahlung mit einem Wellenlängendurchlassband durchzulassen, das einem Absorptionswellenlängenband für die Anregung der genannten Luminophore entspricht, und um Strahlung mit einer Wellenlänge zu blockieren, die einer Emissionswellenlänge der genannten Luminophore entspricht.

4. Vorrichtung nach Anspruch 3, wobei ein Wellenlängendurchlassfilter (54) vor dem Detektor (71) angeordnet ist, um Strahlung mit einer Wellenlänge, die einer Emissionswellenlänge der genannten Luminophore entspricht, durchzulassen und Strahlung, die durch den genannten Bandpassfilter (43) durchgelassen wurde, zu blockieren.

5. Vorrichtung nach einem der vorhergehenden Ansprüche, wobei der Polarisationsfilter einen polarisierenden Strahlteiler (92) umfasst, der Strahlung mit einer Polarisationsebene senkrecht zu der Transmissionsebene der Apertur zu dem genannten Detektor (71) durchlässt und Strahlung mit einer Polarisation parallel zu der Transmissionsebene der Apertur zu einem zweiten Detektor (94) reflektiert oder blockiert.

6. Vorrichtung nach einem der Ansprüche 1 bis 5, wobei die genannte Lichtquelle Licht mit einer niedrigen Kohärenzlänge emittiert, zum Beispiel mit einer Bandbreite von mehr als ca. 1 nm.

7. Vorrichtung nach einem der vorhergehenden Ansprüche, wobei ein Fängermolekül angrenzend an einen Substratendabschnitt der Apertur angeordnet ist, wobei das genannte Fängermolekül dafür vorgesehen ist, ein Aggregat mit dem genannten Zielmolekül und Luminophor zu bilden.

Revendications

1. Dispositif de surveillance du rayonnement émis par des luminophores présents dans un fluide analyte, comprenant :

un biocapteur ayant au moins un matériau non transparent (3) agencé sur un substrat d'un matériau transparent (2) et formant au moins une ouverture (4) destinée à être remplie par un fluide analyte, dans lequel ladite ouverture a une première dimension dans le plan, qui est plus petite que la moitié d'une longueur d'onde de rayonnement efficace dans le biocapteur et une seconde dimension dans le plan qui est plus grande que la moitié d'une longueur d'onde efficace du rayonnement d'excitation, et a un plan de transmission ;

des luminophores immobilisés adjuvants au côté substrat de l'ouverture qui peuvent générer un rayonnement à détecter et des luminophores présents au niveau ou à l'extrémité du côté analyte de l'ouverture qui peuvent générer un arrière-plan indésirable,

une source d'excitation (10, 41) configurée pour émettre un rayonnement d'excitation qui n'est pas polarisé ou polarisé circulairement, elliptiquement ou linéairement comme une combinaison linéaire de lumière d'excitation évanescente et de propagation à l'intérieur de l'ouverture afin d'exciter les luminophores présents dans le fluide analyte dudit biocapteur ;

un bloc d'imagerie (50) comprenant un détecteur (71) permettant de détecter un rayonnement émis par les luminophores lors de l'excitation, et une lentille (51) destinée à diriger le rayonnement émis par les luminophores vers un détecteur (71), ledit bloc d'imagerie (50) étant agencé au niveau d'un côté substrat du biocapteur ;

et un filtre polarisant (53) agencé dans le chemin optique du rayonnement émis par lesdits luminophores entre le biocapteur et le détecteur et à l'extérieur du chemin optique du rayonnement d'excitation, ledit filtre polarisant étant configuré pour supprimer sensiblement la composante de polarisation du rayonnement émis par lesdits luminophores qui est parallèle au plan de transmission de l'ouverture ;

dans lequel le rayonnement d'excitation est dirigé vers le biocapteur à partir du côté substrat à un angle qui est plus grand que l'ouverture numérique de la lentille (51), afin d'être réfléchi dans une direction autre que vers le détecteur.

2. Dispositif selon la revendication précédente, dans lequel ledit filtre polarisant (33, 53) est doté d'une faculté de rotation.

3. Dispositif selon la revendication 1 ou 2, dans lequel ladite source de lumière (41) comprend un filtre passe-bande (43) destiné à faire passer le rayonnement ayant une bande passante de longueur d'onde correspondant à une bande de longueur d'onde d'absorption pour l'excitation desdits luminophores, et à bloquer le rayonnement ayant une longueur d'onde correspondant à une longueur d'onde d'émission desdits luminophores.

4. Dispositif selon la revendication 3, dans lequel un filtre passe-longueur d'onde (54) est agencé avant le détecteur (71) pour faire passer le rayonnement ayant une longueur d'onde correspondant à une longueur d'onde d'émission desdits luminophores et bloquer le rayonnement passé par ledit filtre passe-bande (43).

5. Dispositif selon l'une quelconque des revendications précédentes, dans lequel le filtre polarisant comprend un séparateur de faisceau polarisant (92) faisant passer le rayonnement ayant un plan de polarisation orthogonal au plan de transmission de l'ouverture vers ledit détecteur (71), et réfléchissant ou bloquant un rayonnement ayant une polarisation parallèle au plan de transmission de l'ouverture vers un second détecteur (94).

6. Dispositif selon l'une quelconque des revendications 1 à 5, dans lequel ladite source de lumière émet de la lumière ayant une faible longueur de cohérence, telle qu'ayant une largeur de bande plus grande qu'environ 1 nm.

7. Dispositif selon l'une quelconque des revendications précédentes, dans lequel une molécule de capture est agencée adjacente à une partie d'extrémité de substrat de l'ouverture, ladite molécule de capture étant conçue pour former un agrégat avec ladite molécule cible et ledit luminophore.

Drawing